scholarly journals Catellibacterium nanjingense sp. nov., a propanil-degrading bacterium isolated from activated sludge, and emended description of the genus Catellibacterium

2012 ◽  
Vol 62 (Pt_3) ◽  
pp. 495-499 ◽  
Author(s):  
Jun Zhang ◽  
Shu-An Chen ◽  
Jin-Wei Zheng ◽  
Shu Cai ◽  
Bao-Jian Hang ◽  
...  

A novel facultatively anaerobic, non-spore-forming, non-motile, catalase- and oxidase-positive, Gram-negative and rod-shaped bacterial strain, designated Y12T, was isolated from activated sludge of a wastewater bio-treatment facility. The strain was able to degrade about 90 % of added propanil (100 mg l−1) within 3 days of incubation. Growth occurred in the presence of 0–4.5 % (w/v) NaCl (optimum 0.5 %), at 10–40 °C (optimum 28 °C) and at pH 5.5–10.0 (optimum pH 7.0). Vesicular internal membrane structures and photoheterotrophic growth were not observed. The major respiratory quinone was ubiquinone-10 and the major cellular fatty acid was summed feature 8 (C18 : 1ω6c and/or C18 : 1ω7c). The genomic DNA G+C content of strain Y12T was 63.7 mol%. Phylogenetic analysis based on 16S rRNA gene sequence comparison revealed that strain Y12T was a member of the genus Catellibacterium, as it showed highest sequence similarities to Catellibacterium caeni DCA-1T (99.1 %) and <96.0 % similarities with other species of the genus Catellibacterium. Strain Y12T showed low DNA–DNA relatedness values with C. caeni DCA-1T. Based on phenotypic, genotypic and phylogenetic properties, strain Y12T represents a novel species of the genus Catellibacterium, for which the name Catellibacterium nanjingense sp. nov. is proposed. The type strain is Y12T ( = CCTCC AB 2010218T  = KCTC 23298T). An emended description of the genus Catellibacterium is also presented.

2004 ◽  
Vol 54 (3) ◽  
pp. 955-959 ◽  
Author(s):  
Yasuhiro Tanaka ◽  
Satoshi Hanada ◽  
Akira Manome ◽  
Takayasu Tsuchida ◽  
Ryuichiro Kurane ◽  
...  

A bacterial strain, designated AST4T, was isolated from activated sludge. The bacterium did not show significant growth on nutrient broth, but growth was clearly stimulated by addition of supernatant from other bacterial cultures. Culture filtrate of a strain related to the genus Sphingomonas in particular increased the cell yield and growth rate of strain AST4T. Phylogenetic analysis based on the 16S rRNA gene sequences showed that strain AST4T is located within the ‘Rhodobacter group’ in the α-3 subclass of Proteobacteria, but is clearly distant from related genera in this group such as Paracoccus, Rhodobacter and Rhodovulum. Strain AST4T is a Gram-negative, non-motile, rod-shaped (0·6–0·8×1·3–2·0 μm) and aerobic bacterium. It was not able to reduce nitrate to nitrite or N2. No phototrophic growth was observed. Optimal growth occurred at 30 °C and pH 6·5–7·5. The dominant cellular fatty acid in the isolate was C18 : 1 cis11. Ubiquinone-10 was the major respiratory quinone. The G+C content was 64·5 mol% (by HPLC). Based on the phylogenetic and phenotypic traits, the name Catellibacterium nectariphilum gen. nov., sp. nov. is proposed for this isolate; the type strain is AST4T (=NBRC 100046T=JCM 11959T=DSM 15620T).


Author(s):  
Jia-Yue Zhang ◽  
Xing-Yu Liu ◽  
Shuang-Jiang Liu

A bacterial strain, designated V2M29T, was isolated from forest soil collected in the Changbai Mountains, Heilongjiang Province, China. Cells of strain V2M29T were Gram-positive, rod-shaped (0.5–0.8 μm in diameter and 1.5–2.0 μm in length), strictly aerobic and non-motile. Colonies produced on R2A agar plates were creamy, smooth, circular and 0.3–0.8 mm in diameter. Strain V2M29T grew at 14–35 °C (optimum, 29 °C), at pH 4.1–10.0 (optimum, pH 7.0–8.0) and in the presence of 0–7.0 % (w/v) NaCl (optimum, 0–2.0 %). Strain V2M29T contained MK-8(H4) as the major respiratory quinone and iso-C15 : 0 (20.9 %), iso-C16 : 0 (18.5 %), C17 : 1 ω8c (16.7 %) and 10-methyl-C17 : 0 (9.2 %) as the major cellular fatty acids. The cell-wall peptidoglycan type was based on meso-2,6-diaminopimelic acid and the acyl type of the muramic acid was acetyl. Diphosphatidylglycerol, phosphatidylinositol and six unknown glycolipids were the major polar lipids. The G+C content of the DNA was 72.0 mol% (T m). 16S rRNA gene sequence analysis indicated that strain V2M29T was phylogenetically related to members of the genus Phycicoccus, with sequence similarities ranging from 96.6–97.8 %. The DNA–DNA relatedness values of strain V2M29T to Phycicoccus dokdonensis DS-8T and Phycicoccus bigeumensis DSM 19264T were 32.5±3.3 % and 29.2±2.3 %, respectively. Based on these results, it is concluded that strain V2M29T represents a novel species of the genus Phycicoccus, for which the name Phycicoccus cremeus sp. nov. is proposed, with V2M29T (=CGMCC 1.6963T =NBRC 104261T) as the type strain.


2015 ◽  
Vol 65 (Pt_5) ◽  
pp. 1515-1519 ◽  
Author(s):  
Chao-Yi Lin ◽  
Xi-Ying Zhang ◽  
Ang Liu ◽  
Chang Liu ◽  
Xiao-Yan Song ◽  
...  

A novel Gram-stain-negative, aerobic, orange-pigmented, non-flagellated, gliding, rod-shaped bacterium, designated strain SM1354T was isolated from surface seawater of the Atlantic Ocean. The strain hydrolysed gelatin and DNA but did not reduce nitrate. It grew at 4–40 °C and with 0.5–11 % (w/v) NaCl. Phylogenetic analysis of the 16S rRNA gene sequences revealed that strain SM1354T belonged to the genus Marivirga with 96.0–96.2 % sequence similarities to known species of the genus Marivirga . The major fatty acids of strain SM1354T were iso-C15 : 0, iso-C15 : 1 G, iso-C17 : 03-OH and summed feature 3 (C16 : 1ω7c and/or iso-C15 : 02-OH). Polar lipids of strain SM1354T included phosphatidylethanolamine, three unidentified lipids and one unidentified aminolipid and aminophospholipid. The major respiratory quinone of strain SM1354T was menaquinone 7 (MK-7). The genomic DNA G+C content of strain SM1354T was 33.9±0.4 mol%. On the basis of the results of the polyphasic characterization in this study, it is proposed that strain SM1354T represents a novel species of the genus Marivirga , namely Marivirga atlantica sp. nov. The type strain of Marivirga atlantica is SM1354T ( = CCTCC AB 2014242T = JCM 30305T). An emended description of the genus Marivirga is also proposed.


2015 ◽  
Vol 65 (Pt_10) ◽  
pp. 3256-3261 ◽  
Author(s):  
Chang Liu ◽  
Xi-Ying Zhang ◽  
Xiao-Yan Song ◽  
Hai-Nan Su ◽  
Qi-Long Qin ◽  
...  

A novel Gram-reaction-negative, aerobic, pale-orange-pigmented bacterium, designated strain SM1216T, was isolated from Arctic intertidal sand. Cells of strain SM1216T were dimorphic rods with a single polar prostheca or flagellum. The strain grew at 4 − 30 °C (optimum at 25 °C) and with 0.5 − 6 % (w/v) NaCl (optimum with 2 − 3 %). It reduced nitrate to nitrite but did not hydrolyse gelatin, DNA or Tween 80. Phylogenetic analysis based on 16S rRNA gene sequences revealed that strain SM1216T was affiliated with the genus Algimonas in the family Hyphomonadaceae, sharing 97.5 and 96.3 % similarity with Algimonas ampicilliniresistens 14A-2-7T and Algimonas porphyrae 0C-2-2T, respectively, the two known species in the genus Algimonas. However, the level of DNA–DNA relatedness between strain SM1216T and the type strain of A. ampicilliniresistens, the nearest phylogenetic neighbour, was 57.9 %. The major cellular fatty acids of strain SM1216T were C18 : 1ω7c and C18 : 1 2-OH. The main polar lipids of strain SM1216T were monoglycosyldiglyceride (MGDG), glucuronopyranosyldiglyceride (GUDG), phosphatidylglycerol (PG) and three unidentified phospholipids (PL1–3). The major respiratory quinone was ubiquinone 10 (Q10). The genomic G+C content of strain SM1216T was 60.6 mol%. On the basis of the evidence from this polyphasic study, strain SM1216T represents a novel species in the genus Algimonas, for which the name Algimonas arctica sp. nov. is proposed. The type strain is SM1216T ( = MCCC 1K00233T = KCTC 32513T). An emended description of the genus Algimonas is also given.


2010 ◽  
Vol 60 (1) ◽  
pp. 144-148 ◽  
Author(s):  
Ivone Vaz-Moreira ◽  
Cátia Faria ◽  
Ana R. Lopes ◽  
Liselott A. Svensson ◽  
Edward R. B. Moore ◽  
...  

A bacterium, designated strain DC-196T, isolated from kitchen refuse compost was analysed by using a polyphasic approach. Strain DC-196T was characterized as a Gram-negative short rod that was catalase- and oxidase-positive, and able to grow at 10–40 °C, pH 6–9 and in NaCl concentrations as high as 3 %. Chemotaxonomically, C18 : 1 was observed to be the predominant cellular fatty acid and ubiquinone 10 (Q10) was the predominant respiratory quinone. The G+C content of the genomic DNA was determined to be 66 mol%. On the basis of the genotypic, phenotypic and chemotaxonomic characteristics, strain DC-196T was assigned to the genus Shinella, although with distinctive features. At the time of writing, 16S rRNA gene sequence similarities of 97.6–96.8 % and the low DNA–DNA hybridization values of 38.2–32.2 % with the type strains of the three recognized Shinella species confirmed that strain DC-196T represents a novel species of the genus, for which the name Shinella fusca sp. nov. is proposed (type strain DC-196T=CCUG 55808T=LMG 24714T).


2006 ◽  
Vol 56 (11) ◽  
pp. 2693-2695 ◽  
Author(s):  
Xing-Yu Liu ◽  
Bao-Jun Wang ◽  
Cheng-Ying Jiang ◽  
Shuang-Jiang Liu

Bacterial strain LW36T was isolated from activated sludge of a wastewater-treatment bioreactor. Cells of strain LW36T were Gram-negative coccoids to short rods, 1.0–1.2×0.5 μm in size. Colonies were cream-coloured, smooth and circular. Strain LW36T was hetero-organotrophic and chemolithotrophic and was able to use reduced sulfur as an energy resource. Growth was observed at 25–36 °C and pH 5–10. The most abundant cellular fatty acid of strain LW36T was C18 : 1 ω7c (64.2 %). The sole respiratory quinone was ubiquinone-10. The G+C content of the genomic DNA was 61.3 mol% (T m). 16S rRNA gene sequence analysis indicated that strain LW36T was phylogenetically related to members of the genus Paracoccus, with similarities ranging from 92.4 to 94.9 %. Based on these results, it is concluded that strain LW36T represents a novel species of the genus Paracoccus, for which the name Paracoccus sulfuroxidans is proposed. The type strain is strain LW36T (=CGMCC 1.5364T=JCM 14013T).


Author(s):  
Xiuqing Xue ◽  
Kundi Zhang ◽  
Feng Cai ◽  
Jun Dai ◽  
Yang Wang ◽  
...  

A Gram-negative, rod-shaped, non-motile, strictly aerobic bacterium, strain S3-63T, was isolated from desert sand of Xinjiang, China. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain S3-63T had highest similarity to type strains of the genus Altererythrobacter, i.e. Altererythrobacter marinus H32T (97.2 % similarity), Altererythrobacter marensis MSW-14T (95.9 %), Altererythrobacter aestuarii KCTC 22735T (95.5 %), Altererythrobacter epoxidivorans JCS350T (95.1 %), Altererythrobacter namhicola KCTC 22736T (95.1 %), Altererythrobacter luteolus SW-109T (95.0 %) and Altererythrobacter indicus LMG 23789T (93.5 %). Growth occurred at 20–37 °C (optimum 30 °C), at pH 7.0–9.0 (optimum pH 8.0) and in 0–3 % (w/v) NaCl (optimum 1 %). The major respiratory quinone was ubiquinone-10 and the predominant cellular fatty acids were C18 : 1ω7c (50.8 %), summed feature 3 (C16 : 1ω7c and/or C16 : 1ω6c; 12.6 %), C16 : 0 (12.3 %), C14 : 0 2-OH (7.3 %) and C17 : 1ω6c (4.5 %). The DNA G+C content was 64.6 mol%. Therefore, the phylogenetic, physiological and chemotaxonomic data demonstrated that strain S3-63T represents a novel species of the genus Altererythrobacter, for which the name Altererythrobacter xinjiangensis sp. nov. is proposed; the type strain is S3-63T ( = CCTCC AB 207166T = CIP 110125T). An emended description of the genus Altererythrobacter is provided.


2011 ◽  
Vol 61 (8) ◽  
pp. 1921-1926 ◽  
Author(s):  
Jin-Wei Zheng ◽  
Yi-Guang Chen ◽  
Jun Zhang ◽  
Ying-Ying Ni ◽  
Wen-Jun Li ◽  
...  

A novel non-sporulating, non-motile, catalase- and oxidase-positive, strictly aerobic, Gram-negative, rod-shaped bacterial strain, designated DCA-1T, was isolated from activated sludge collected from a butachlor wastewater treatment facility. The strain was able to degrade about 85 % of 100 mg butachlor l−1 within 5 days of incubation. Growth occurred in the presence of 0–6 % (w/v) NaCl [optimum, 1 % (w/v) NaCl] and at pH 5.5–9.0 (optimum, pH 7.0) and 15–35 °C (optimum, 25–30 °C). Vesicular internal membrane structures and photoheterotrophic growth were not observed. The major respiratory quinone was ubiquinone 10 (Q-10) and the major cellular fatty acids were C18 : 1ω7c and 11-methyl C18 : 1ω7c. The genomic DNA G+C content of strain DCA-1T was 62.5 mol%. Phylogenetic analysis based on 16S rRNA gene sequence comparison revealed that strain DCA-1T was a member of the family Rhodobacteraceae and was related most closely to the type strain of Catellibacterium aquatile (96.5 % sequence similarity). The combination of phylogenetic analysis, phenotypic characteristics and chemotaxonomic data supports the suggestion that strain DCA-1T represents a novel species of the genus Catellibacterium, for which the name Catellibacterium caeni sp. nov. is proposed. The type strain is DCA-1T ( = CGMCC 1.7745T  = DSM 21823T). In addition, based on the characterization data obtained in this study, it is proposed that Rhodobacter changlensis should be reclassified as Catellibacterium changlense comb. nov. (type strain JA139T  = DSM 18774T  = CCUG 53722T  = JCM 14338T). An emended description of the genus Catellibacterium is also presented.


2013 ◽  
Vol 63 (Pt_5) ◽  
pp. 1766-1770 ◽  
Author(s):  
Joon Yong Kim ◽  
Jina Lee ◽  
Na-Ri Shin ◽  
Ji-Hyun Yun ◽  
Tae Woong Whon ◽  
...  

A novel Gram-stain-negative, facultatively anaerobic, non-motile and coccus-shaped bacterium, strain C7T, was isolated from the gut of the butterfly Sasakia charonda. Strain C7T grew optimally at 20–25 °C, at pH 7–8 and with 1 % (w/v) NaCl. The strain was negative for oxidase activity but positive for catalase activity. The 16S rRNA gene sequences of strain C7T and Orbus hercynius CN3T shared 96.8 % similarity. The major fatty acids identified were C14 : 0, C16 : 0, C18 : 1ω7c and summed feature 2 (comprising C14 : 0 3-OH/iso-C16 : 1). The major respiratory quinone was ubiquinone-8 (Q-8). The polar lipids of strain C7T were phosphatidylethanolamine, phosphatidylglycerol, an unidentified phospholipid and two unidentified aminophospholipids. The G+C content of the genomic DNA extracted from strain C7T was 32.1 mol%. Taken together, the phenotypic, genotypic and phylogenetic analyses indicate that strain C7T represents a novel species of the genus Orbus , for which the name Orbus sasakiae sp. nov. is proposed. The type strain is C7T ( = KACC 16544T = JCM 18050T). An emended description of the genus Orbus is provided.


2011 ◽  
Vol 61 (11) ◽  
pp. 2734-2739 ◽  
Author(s):  
Chae-Sung Lim ◽  
Yong-Sik Oh ◽  
Jae-Kwan Lee ◽  
A-Rum Park ◽  
Jae-Soo Yoo ◽  
...  

A yellow-pigmented, Gram-staining-negative, non-motile, strictly aerobic and rod-shaped bacterium, designated CS100T, was isolated from soil in Chungbuk, Korea. Phylogenetic analysis and comparative studies based on the 16S rRNA gene sequence showed that strain CS100T belonged to the genus Flavobacterium in the family Flavobacteriaceae. Strain CS100T showed the highest sequence similarities to Flavobacterium glaciei JCM 13953T (97.6 %) and Flavobacterium johnsoniae KACC 11410T (97.1 %). Sequence similarity to other members of the genus Flavobacterium was 91.5–97.0 %. Growth occurred at 4–30 °C, at pH 5.0–9.0 and in the presence of 0–2 % (w/v) NaCl. Flexirubin-type pigments were produced. Menaquinone-6 (MK-6) was the major respiratory quinone and the major fatty acids were iso-C15 : 0 (17.3 %), summed feature 3 (comprising iso-C15 : 0 2-OH and/or C16 : 1ω7c, 15.5 %) and C16 : 0 (11.8 %). The DNA G+C content was 36.4 mol%. Strain CS100T hydrolysed skimmed milk and gelatin, but not chitin or pectin, and showed oxidase and catalase activities. DNA–DNA relatedness was 3.0 % with F. glaciei JCM 13953T and 11.5 % with F. johnsoniae KACC 11410T. On the basis of the evidence from this study, strain CS100T represents a novel species of the genus Flavobacterium, for which the name Flavobacterium chungbukense sp. nov. is proposed. The type strain is CS100T ( = KACC 15048T = JCM 17386T).


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